Takes a VCF and infers annotations and variant effects from a GFF using SnpEff.
SnpEff is a tool that annotates and predicts the effects of variants on genes. SnpEffWrapper takes a VCF and, using SnpEff, infers annotations and variation effects from a GFF. If you use SnpEffWrapper, please consider citing SnpEff. This software is not endorsed in any respect by the original authors.
SnpEffWrapper has the following dependencies:
- SnpEff (>= 4.1)
- Java (>= 1.7)
- Jinja2
- PyVCF
- PyYAML
Details for the installation are provided below. If you encounter an issue when installing SnpEffWrapper please contact your local system administrator. If you encounter a bug please log it here or email us at [email protected]
Install snpEff and Java 1.7 then
pip install git+https://github.com/sanger-pathogens/SnpEffWrapper.git
The test can be run from the top level directory:
./snpEffWrapper/tests/test_wrapper.py
$ snpEffBuildAndRun --help
usage: snpEffBuildAndRun [-h] [--snpeff-exec SNPEFF_EXEC]
[--java-exec JAVA_EXEC] [--coding-table CODING_TABLE]
[-o OUTPUT_VCF] [--debug] [--keep]
gff_file vcf_file
Takes a VCF and applies annotations from a GFF using SnpEff
positional arguments:
gff_file GFF with annotations including a reference genome
sequence
vcf_file VCF input to annotate (NB must be aligned to the
reference in your GFF
optional arguments:
-h, --help show this help message and exit
--snpeff-exec SNPEFF_EXEC
Path to your prefered SnpEff executable (default:
snpEff.jar)
--java-exec JAVA_EXEC
Path to Java 1.7 (default: java)
--coding-table CODING_TABLE
A mapping of contig name to coding table formatted in
YAML
-o OUTPUT_VCF, --output_vcf OUTPUT_VCF
Output for the annotated VCF (default: stdout)
--debug Show lots of SnpEff and other debug output
--keep Keep temporary files and databases (useful for
debugging)
- snpEffBuildAndRun will look for SnpEFF.jar in the following locations:
- the file specified by
--snpeff-exec
snpEff.jar
in your local directorysnpEff.jar
in yourPATH
- the file specified by
- SnpEff needs Java 1.7 to run; snpEffBuildAndRun will look in the following locations:
- the file specified by
--java-exec
java
in yourPATH
- the file specified by
$ snpEffBuildAndRun snpEffWrapper/tests/data/minimal.gff snpEffWrapper/tests/data/minimal.vcf -o minimal.annotated.vcf
You can provide a coding table for each VCF contig otherwise it'll default to SnpEff's 'Bacterial_and_Plant_Plastid'. You can do this by providing a mapping for each contig in your VCF to the relevant table in snpEffWrapper/data/config.template in YAML format.
For example:
snpEffBuildAndRun minimal.gff minimal.vcf \
--coding-table 'default: Standard'
snpEffBuildAndRun minimal.gff minimal.vcf \
--coding-table '{CHROM1: Standard, MITO1: Mitochondrial}'
snpEffBuildAndRun minimal.gff minimal.vcf \
--coding-table '{default: Standard, MITO1: Mitochondrial}'
NB you don't need curly brackets if you're only mapping one contig (or setting a default); you do need them if you're setting different coding tables.
- The GFF must contain the reference sequence in Fasta format
- The VCF must be aligned against the reference in the GFF
- At least one of the contigs in the VCF must have annotation data in the GFF (you'll get warnings for each VCF config not in the GFF)
- You cannot provide unknown coding tables (i.e. that can't be found in config.template)
SnpEffWrapper is free software, licensed under GPLv3.
Please report any issues to the issues page or email [email protected].
If you use this, please consider citing SnpEff. This software is not endorsed in any respect by the original authors.